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Dive into the research topics where Sanghee Kim is active.

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Featured researches published by Sanghee Kim.


Tetrahedron Letters | 2001

Enantioselective syntheses of (+)-decursinol and (+)-trans-decursidinol

Sanghee Kim; Hyojin Ko; Soonjoo Son; Kye Jung Shin; Dong Jin Kim

Abstract Selective and practical asymmetric syntheses of (+)-decursinol ( 1 ) and (+)- trans -decursidinol ( 2 ) have been achieved using naturally occurring umbelliferone, demethylsuberosin, and xanthyletin as the synthetic intermediates. The absolute stereochemistry was established in the late stage of synthesis by employing Jacobsens enantioselective epoxidation conditions.


Tetrahedron Letters | 2003

Total synthesis and determination of the absolute configuration of (+)-neoisoprelaurefucin

Hyunjoo Lee; Hyoungsu Kim; Seungyoup Baek; Sanghee Kim; Deukjoon Kim

The first total synthesis of the seven-membered ring ether marine natural product (+)-neoisoprelaurefucin (1) has been achieved employing a regioselective internal alkylation of amide 3, a novel sequence for removal of the triethylsilyl group from the resulting triethylsilyloxepene 2, and a bromoetherification of alcohol 16 as key steps. In addition, the absolute stereochemistry of the natural product was assigned.


Tetrahedron Letters | 2003

Efficient construction of bicyclic systems by an internal SN2′ enolate alkylation/ring-closing metathesis (RCM) strategy: a concise synthesis of the trans-hydrindane nucleus

Hyunil Jo; Jongkook Lee; Hyoungsu Kim; Sanghee Kim; Deukjoon Kim

Abstract A concise and efficient synthesis of the trans-hydrindane system has been achieved by a novel intramolecular SN2′ enolate alkylation/ring-closing metathesis (RCM) strategy with a good degree of stereocontrol.


Tetrahedron Letters | 2002

Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect

Won Jun Choi; Hee Sung Ahn; Hea Ok Kim; Sanghee Kim; Moon Woo Chun; Lak Shin Jeong

Abstract Novel amino-substituted apio nucleoside (2R,4R)-LJ-45 as a potential anti-HBV agent was stereoselectively synthesized from the known oxazolidine 1 through a distant neighboring group effect. It is believed that this synthetic method using a chiral template, (−)- l -serine methyl ester can be generally applied to the synthesis of other chiral amino-substituted nucleosides.


Materials Science Forum | 2016

Influence of Impurities in SiC Powder on High Quality SiC Crystal Growth

S. Heo; H.R. Son; Byung Sook Kim; Kim; Jung Eun Han; Dong Hoon Lee; K. S. Min; Sanghee Kim; S. Ha; Dong Geun Shin

SiC powders having different purities were prepared by carbothermal reduction under different conditions from traditional process and SiC single crystals were grown by the PVT method from the powders. After crystal growth, boule was cut to wafers and they were polished for chemical and defect analyses. Total impurities including Al, B and Ti which were derived from powders decreased remarkably during crystal growth. The formation of defects including micropipe and dislocations such as TED, TSD and BPD was strongly influenced by impurity content. The effect of impurity seemed to be negligible at below 1ppm level for MPD. On the other hand, dislocations continuously decreased even more when higher purity SiC powder below 1ppm level was used.


Angewandte Chemie | 2010

Substrate-Controlled Asymmetric Total Synthesis and Structure Revision of (+)-Itomanallene A†

Wonjang Jeong; Mi Jung Kim; Hyoungsu Kim; Sanghee Kim; Deukjoon Kim; Kye Jung Shin


Angewandte Chemie | 2007

Substrate-Controlled Asymmetric Total Synthesis of (+)-Microcladallene B with a Bromination Strategy Based on a Nucleophile-Assisting Leaving Group†

Janghyun Park; Byungsook Kim; Hyoungsu Kim; Sanghee Kim; Deukjoon Kim


Angewandte Chemie | 2011

Simple Determination of Double‐Bond Positions in Long‐Chain Olefins by Cross‐Metathesis

Yongseok Kwon; Seon-Woo Lee; Dong-Chan Oh; Sanghee Kim


Angewandte Chemie | 2009

Synthesis and Structural Analysis of One‐Dimensional sp‐Hybridized Carbon Chain Molecules

Sanghee Kim


Synthesis | 2003

Efficient Syntheses of Biologically Important ( S)-2-Amino-8-oxodecanoic Acid (Aoda) and Homologues

Sanghee Kim; Eun-Young Kim; Hyojin Ko; Young Hoon Jung

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Deukjoon Kim

Seoul National University

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Hyojin Ko

Seoul National University

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Kye Jung Shin

Korea Institute of Science and Technology

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Seon-Woo Lee

Seoul National University

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Byungsook Kim

Seoul National University

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Dong Jin Kim

Korea Institute of Science and Technology

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Dong-Chan Oh

Seoul National University

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